SUPPORTED MO-O-K-MExOy CATALYST FOR THE SYNTHESIS OF METHANETHIOL FROM HIGH H2S-CONTAINING SYNGAS

ABSTRACT

This invention is related to a preparation method of a supported catalyst Mo—O—K-Me x O y  for the synthesis of methanethiol from H 2 S-containing syngas. The catalyst comprises of an active component of Mo—O—K-based species, an active promoter and a support denoted as metal (or metals)-carrier. The support is prepared by electroless plating method in such a way that the metal or metals chosen are plated onto the surface of the carrier. Transition metal, especially Fe, Co or Ni are selected to be the plating metal, while SiO 2 , Al 2 O 3  or TiO 2  are selected to be carrier. The catalyst thus prepared is found to be efficient for the synthesis of methanethiol from H 2 S-containing syngasor carbon oxides/hydrogen mixtures, especially regarding a minor formation of the by-product CO 2 .

The present invention relates to a preparation method of a supported Mo—O—K-Me_(x)O_(y) catalyst for the synthesis of methanethiol from high H₂S-containing syngas, therein support is a metal (or metals)-plated carrier, especially metal (or metals)-plated-SiO₂, which is made by electroless plating method.

THE PRIOR ART

As an important chemical material used to produce methionine, pesticides and medicine, methanethiol is predominantly prepared by the reaction of hydrogen sulfide with methanol. The direct synthesis of methanethiol from the reaction of H₂S with carbon oxides, in particular, from H₂S-containing syngas is an attractive alternative. For example, EP167,354 disclosed a synthesis pathway from the reaction of hydrogen sulfide with carbon monoxide in the presence of a catalyst NiO or MoO₃ supported on TiO₂; Chinese patent CN98118186.4 and CN98118187.2 disclosed Mo—S—K/SiO₂ catalysts used for methanethiol synthesis from high H₂S-containing syngas; Chinese patent appl.200310100496.1 and 200310100495 reported Mo—O—K/SiO₂ catalysts promoted by transition metal oxides or rare earth metal oxides for the methanethiol synthesis, herein the promoters were selected from the oxides of Co, Ni, Fe, Mn or the rare earth oxides of La, Ce, the active component Mo—O—K base are formed from the precursor K₂MoO₄ or (NH₄)₆Mo₇O₂₄.4H₂O plus potassium salt. Those catalysts were prepared by traditional impregnation method. The catalysts exhibit high selectivity and space-time-yield of methyl mercaptan, but produce also by-products, such as carbonyl sulfide, methane and dimethyl sulfide.

STATEMENT OF THE INVENTION

The object of this invention is to develop a further improved solid supported Mo—O—K-Me_(x)O_(y) catalyst with high activity and selectivity of methanethiol, but lower selectivity of CO₂.

DETAILED DESCRIPTION OF THE INVENTION

The object of the invention is a catalyst comprising:

-   a) a support, consisting of a porous carrier and a metal A deposited     thereon by electroless deposition of metal on the carrier; -   b) a Mo—O—K based active component; and -   c) optionally an active promoter Me_(x)O_(y), chosen from the group     of transition metal oxides or rare earth metal oxides or rare earth     metal oxides, wherein x and y depend on the valence of the metal.

The catalyst comprises an active component, optionally an active promoter and a support. Said active component is a Mo—O—K-based component. Said promoter is at least one chosen from the group of transition metal oxides, or rare earth metal oxides, comprising especially from the oxides of iron, cobalt, Nickel, manganese, lanthanum and cerium, and expressed as Me_(x)O_(y), wherein “Me” denotes the metal selected from the group of transition metals of rare earth metals, especially Fe, Co, Ni, Mn, La or Ce.

Said support is a metal (or metals)-plated carrier, especially metal (or metals)-SiO₂, which is made by electroless plating method. In general the carrier used is porous and chosen from the group of SiO₂, Al₂O₃, TiO₂, Zeolites, especially SiO₂. Said metal or metals plated on said carrier can be selected from the group of Ni, Co or Fe, preferably Ni or Co.

When potassium molybdate is used as precursor of the Mo—O—K-based component, the catalyst of present invention is denoted as K₂MoO₄-Me_(x)O_(y)/Metal-carrier, wherein the weight ratios of the components of the catalyst are

K₂MoO₄/Me_(x)O_(y)/metal-carrier=(1-30)/(0.0-25.0)/(0.1-10.0)-100, preferably (15-20)/(0.0-25.0)/(0.5-8.0)-100;

when (NH₄)₆Mo₂O₂₄.4H₂O plus one of potassium salts or MoO₃ plus one of potassium salts serve as precursors of the Mo—O—K-based compound, the catalyst of the present invention is expressed as MoO₃—K₂O-Me_(x)O_(y)/metal-carrier, wherein the weight ratios of the components of the catalyst are: MoO₃/K₂O/Me_(x)O_(y)/metal-carrier=(1-30)/(1-20)/(0.0-25.0)/(0.1-10.0)-100, preferably (15-20)/(10-15)/(0.0-25.0)/(0.5-8.0)-100; Said potassium compound is at least one chosen from the group, comprising

K₂CO₃, KOH, KNO₃ and CH₃COOK.

Chemically metal-plating method is used to prepare said metal (or metals)-carrier the metal (or metals) chosen is plated onto the carrier chosen, wherein the weight ratio of metal (or metals)/carrier is (0.1-10.0)/100, preferably (0.5-8.0)/100.

The invention is also directed to the preparation of said catalysts by multi-step impregnation.

In order to distribute the active component more equally over the support, at least one chelating reagent should be used in the impregnation process.

Said chelating or coordinating reagent is at least one chosen from the group comprising citric acid, ammonium citrate, L-glutamic acid, tartaric acid and ethylenediaminetetraacetic acid(EDTA); the amount of chelating agent added correspondingly is 0.1-0.6 times as much by weight as that of the support, more preferably is 0.3-0.6 times as much as that of the support. Suitable amounts of ammonia are added to adjust the pH value of the steeping liquor to 7.0-13.0, preferable 8.0-12.0.

The activation of the carrier by chemically plating metal proceeds as follows (shown as a preferred method):

-   (1) the preparation of metal-plating solution:     -   A given quantity of soluble metal salt chosen and a given         quantity of coordinating agent are dissolved in a given quantity         of distilled water successively to produce a metal-plating         solution, in which the concentration of the metal ions varies         from 1 g/l to 20 g/l, preferably 5-7 g/l; the coordinating agent         is at least one chosen from Na₃C₆H_(S)O₇.2H₂O, C₆H₈O₇.H₂O,         C₂H₈N₂ or NaKC₄H₄O₆.4H₂O, the concentration of the coordinating         agent varies from 1 g/l to 20 g/l.     -   Keeping stirring for 10 minutes, then a given quantity of the         stabilizing agents (NH₄)₂SO₄ or Na₃C₆H_(S)O₇.2H₂O, is added         subsequently to the plating solution obtained above followed by         stirring for another 20 minutes, followed by adding some NH₃.H₂O         to adjust the pH of the plating solution to 7.0-13.0, preferably         8.0-12.0; finally, a suitable amount of distilled water is added         to adjust the volume of the solution in such a way that the         concentration of metal salt chosen in the plating solution         varies from 1 g/l to 20 g/l, preferably 5-7 g/l. -   (2) Pretreatment of the carrier:     -   Prior to plating the metal onto the carrier, the carrier is         preferably pretreated by the following processes:     -   a) the carrier should be washed with distilled water, and then         dried, followed by immersing the clean carrier in a solution of         4.5 mol/1H₂SO₄+0.88 mol/1H₂O₂ (1:1) for 5 minutes under         agitating, and subsequently washed with distilled water three         times;     -   b) the cleaned carrier is immersed in an aqueous solution of         activation agent under agitation, said activation agent is         preferably PdCl₂/HCl, the concentration of the activation agent         varies in general from 0.05 g/l to 1.0 g/l, preferably from 0.1         g/l to 0.5 g/l; keeping ultrasonically agitating for e.g. 30-35         minutes, then washing with distilled water three times;     -   c) the activated carrier is immersed in an aqueous solution of a         reducing agent under agitation; the reducing agent is preferably         NaH₂PO₄ or NaBH₄; the concentration of the agent varies from 20         g/l to 30 g/l; -   (3) Plating of metal onto carrier is conducted by putting the     pretreated carrier produced in step (2) into the plating solution of     the metal chosen at 40-85° C. for 30-40 minutes. The metal-platted     carrier is washed with distilled water e.g. for three times and then     dried at about 110° C. for about 6 hours. The metal-plated carrier     is termed support, such as support Ni—SiO₂ or Co—SiO₂.     Impregnation of the Support with the Active Component (Shown as a     Preferred Method)

(1) A given quantity of said precursor K₂MoO₄ or (NH₄)₆Mo₇O₂₄ plus a potassium salt or MoO₃ plus a soluble potassium compound and suitable amount of chelating agent are dissolved in distilled water to generate an impregnation solution; into which then a suitable amount of NH₃.H₂O is dropped to adjust the pH of the impregnation solution at 8-12, preferably 8-10; then the metal-plated carrier (30-45 meshes) produced in step (3) of carrier activation is soaked in the impregnation solution at room temperature for 12 hours, then dried at 120° C. for 5 hours to produce the desired supported Mo—O—K catalyst.

(2) Alternatively, a given quantity of said precursor K₂MOo₄ or (NH₄)₆Mo₇O₂₄ plus a soluble potassium compound or MoO₃ plus a potassium salt are dissolved in distilled water, then a suitable amount of NH₃.H₂O is dropped into the solution to make the precursor fully dissolved in the distilled water to generate an impregnation solution, which contains only an active component.

In a preferred case a given quantity of soluble transition metal salt or rare earth metal salt chosen, especially, its sulfate, nitrate or acetate, and suitable amount of chelating agent are added to the above described solution, into which a suitable amount of NH₃.H₂O is then dropped to adjust the pH of the impregnation solution at 8-12, preferably 8-10; lastly the metal (or metals)-plated carrier (30-45 meshes) produced in step (3) of carrier activation is soaked in the impregnation solution at room temperature for 12 hours, then filtered and dried at 110° C. for 6 hours to produce the desired supported Mo—O—K-Me_(x)O_(y) catalyst.

Said catalyst is used for a method to prepare methanethiol from high H₂S-containing syngas. The reaction conditions are known from the state of art.

The catalyst should be sulfided for 8-10 h before using.

The reactivity evaluation of the catalyst of present invention was carried out in a fixed-bed tubular reactor with 0.5 ml of catalyst per pass. The reaction conditions are preferably CO/H₂/H₂S=1/1/2, 250-350° C., about 0.05-0.3 MPa and GHSV=500-3000 h⁻¹. The products were analyzed by GC. All date were taken after the steady state achieved.

The assay results show that the catalyst of the present invention were not only has high catalytic activity for the synthesis of methanethiol from high H₂S-containing syngas, but also has high selectivity of methanethiol, but less selectivity of CO₂.

The following examples illustrate the present invention further.

Example 1 Electroless Plating

(1) 2.0 g of NiSO₄.7H₂O and 2.0 g of Na₃C₆H_(S)O₇.2H₂O were dissolved in 50 ml of distilled water successively to produce a plating solution, keeping stirring for 10 minutes, then 3.0 g of (NH₄)₂SO₄ and 3.0 g of NaH₂PO₄.H₂O were added one after another to the solution obtained above, stirring for another 20 minutes, followed by adding some NH₃.H₂O to adjust the pH of the solution to 9.0; finally, distilled water was added to adjust the volume of the solution to 100 ml in such a way that the concentration of NiSO₄ in the plating solution is 20 g/l;

(2) 10 g of clean SiO₂ was immersed in 20 ml of 4.5 mol/l H₂SO₄+0.88 mol/l H₂O₂(1:1) solution for 5 minutes under agitating, and then washed for three times with distilled water; followed by immersing the carrier SiO₂ in 20 ml of 0.1 g/l PdCl₂/HCl solution, keeping ultrasonically agitating for 30 minutes, and then washed for three times with distilled water; the next step was to immerse the activated carrier SiO₂ in 10 ml of 30 g/l NaH₂PO₄ solution, at the same time agitating for 10 seconds and repeated the reduced experiment step again, so as to form an activated carrier.

(3) The electroless plating process was carried out by immersing the activated carrier SiO₂ in the plating solution prepared in step (2) at appr. 40° C. for 30 minutes. After plating, the Ni-plated SiO₂ was washed with distilled water three times and dried at 383K for 4 h. The weight ratio of metal over carrier of the support thus prepared was Ni—SiO₂=4.4-100.

(4) 0.45 g of K₂MoO₄ and 3.0 g of tartaric acid were dissolved in 6 ml of distilled water to generate an impregnation solution, into which then 0.8 ml of NH₃.H₂O was dropped to adjust the pH of the impregnation solution at 9. Then 3 g of support Ni—SiO₂ (30-45 meshes) produced in step (3) was soaked in the impregnation solution at room temperature for 12 hours, then dried at 110° C. for 5 hours. The weight ratio of every component of the catalyst was K₂MoO₄/Ni—SiO₂=15/(4.4-100). The evaluation result of the catalyst thus prepared is shown in table 1.

Example 2, 3, 4

The catalysts were prepared according to the experiment steps described in Example 1, but the concentration of the plating solution was respectively diluted by once, twice three times with distilled water, namely the nickel ion concentration was respectively 10 g/1, 6.67 g/1, 5 g/l. The weight ratio of every content of the catalysts gained was K₂MoO₄/Ni—SiO₂=15/(2.2-100), K₂MoO₄/Ni—SiO₂=15/(1.5-100), K₂MoO₄/Ni—SiO₂=15/(1.1-100) respectively. The evaluation results of the catalysts thus prepared were also shown in table 1.

Example 5, 6

The catalysts were prepared according to the experiment steps described in Example 1, but the weight of carrier SiO₂ to be plated was respectively 8 g and 6 g. The weight ratio of every content of the catalysts gained was K₂MoO₄/Ni—SiO₂=15/(5.5-100) and K₂MoO₄/Ni—SiO₂=15/(7.3-100), respectively. The evaluation results of the catalysts thus prepared are also shown in table 1.

TABLE 1 performance of the catalysts K₂MoO₄/Ni—SiO₂ in examples 1-6 selectivity CO % examples K₂MoO₄/Ni—SiO₂ CH₄ CH₃SH COS CO₂ CO₂/CH₃SH conversion 1 15/(4.4-100) 0.0226 46.84 18.91 34.02 0.7265 56.84 2 15/(2.2-100) 0.0216 46.31 20.33 33.14 0.7156 63.45 3 15/(1.5-100) 0.0202 46.61 20.67 32.70 0.7017 65.61 4 15/(1.1-100) 0.0130 43.37 24.91 31.70 0.7311 49.16 5 15/(5.5-100) 0.0207 46.70 19.01 34.27 0.7338 56.57 6 15/(7.3-100) 0.0196 46.85 19.14 34.99 0.7255 55.46

Example 7, 8, 9, 10, 11

The catalysts were prepared according to the experiment steps described in Example 3, but the weight ratio of K₂MoO₄/support varied from 5/100, 10/100, 15/100, 20/100, 25/100. The weight ratio of every component of the catalysts gained was K₂MoO₄/Ni—SiO₂=5/(1.5-100), K₂MoO₄/Ni—SiO₂=10/(1.5-100), K₂MoO₄/Ni—SiO₂=15/(1.5-100), K₂MoO₄/Ni—SiO₂=20/(1.5-100), K₂MoO₄/Ni—SiO₂=25/(1.5-100) respectively. The evaluation results of the catalysts thus prepared were also shown in table 2.

Example 12

(1) 0.667.0 g of NiSO₄.7H₂O and 0.667 g of Na₃C₆H_(S)O₇.2H₂O were dissolved into 50 ml of distilled water successively to produce a plating solution, keeping stirring for 10 minutes, then 1.0 g of (NH₄)₂SO₄ and 1.0 g of NaH₂PO₄.H₂O were added one after another to the solution obtained above, stirring for another 20 minutes, followed by adding some NH₃.H₂O to adjust the pH of the solution to 9.0; finally, distilled water was added to adjust the volume of the solution to 100 ml in such a way that the concentration of NiSO₄ in the plating solution was 4.12 g/l;

(2) 10 g of clean SiO₂ were immersed in 20 ml of 4.5 mol/l H₂SO₄+0.88 mol/l H₂O₂(1:1) solution for 5 minutes under agitating, and then washed for three times with distilled water, followed by immersing the carrier SiO₂ in 20 ml of 0.1 g/l PdCl₂/HCl solution, at the same time keeping ultrasonically agitating for 30 minutes, and then washed for three times with distilled water; the next step was to immerse the activated carrier SiO₂ in 10 ml of 30 g/l NaH₂PO₄ solution, at the same time agitating for 10 seconds; finely repeated the reduced experiment step again to produce an activated carrier SiO₂.

(3) The electroless plating process was carried out by immersing the activated carrier SiO₂ in the plating solution prepared in step (2) at 42° C. for 30 minutes. After plating, the Ni-plated SiO₂ was washed with distilled water four times and then dried at 110° C. for 6 hours. The weight ratio of the two contents of the support thus prepared was Ni—SiO₂=1.5-100.

(4) 0.496 g of K₂MoO₄ and 1.0 ml of NH₃.H₂O were dissolved in 5 ml of distilled water to generate an impregnation solution; then 0.5 g of tartaric acid and 0.135 g of Ni(NO₃)₂₋₆H₂O were added to the K₂MoO₄ solution, the pH value of the K₂MoO₄ solution was measured to be at 9; then 3 g of support nickel-plated SiO₂ (30-45 meshes) produced in step (3) was soaked in the impregnation solution at room temperature for 12 hours, then dried at 110° C. for 6 hours. The weight ratio of every component of the catalyst thus prepared was K₂MoO₄/NiO/Ni—SiO₂=15/1.0/(1.5-100). The evaluation result of the catalyst thus prepared is shown in table 3.

Example 13

The catalyst was prepared according to the experiment steps described in Example 12, but 0.1346 g of Co (NO₃)₂₋₆H₂O substituted for 0.135 of Ni(NO₃)₂₋₆H₂O. The weight ratio of every component of the catalyst thus prepared was K₂MoO₄/CoO/Ni—SiO₂=15/1.0/(1.5-100). The evaluation result of the catalyst thus prepared is also shown in table 3

Example 14

The catalyst was prepared according to the experiment steps described in Example 1, but NiSO₄.7H₂O for preparing plating solution was replaced by CoSO₄.7H₂O, the amount of CoSO₄.7H₂O is the same as that of NiSO₄.7H₂O, but the Ph value of the plating solution was adjusted by NH₃.H₂O to 12; the plating process of the activated carrier SiO₂ was carried out at 80° C. The weight ratio of every component of the catalyst gained was K₂MoO₄/(Co—SiO₂)=15/(4-100). The evaluation result of the catalyst thus prepared was shown in table 4

Example 15

The catalyst was prepared according to the experiment steps described in Example 12, but 0.667 g of NiSO₄.7H₂O for preparing plating solution was replaced by 0.667 g of CoSO₄.7H₂O; while the quantity of Ni(NO₃)₂₋₆H₂O for preparing promoter Me_(x)O_(y) was 0.117 g. The weight ratio of every component of the catalyst gained was K₂MoO₄/NiO/Co—SiO₂=15/1/(1.5-100). The evaluation result of the catalyst thus prepared is also shown in table 4

Example 16

The catalyst was prepared according to the experiment steps described in Example 15, but 0.117 g of Ni(NO₃)₂.6H₂O for preparing promoter Me_(x)O_(y) was replaced by 0.117 g of Co(NO₃)₂₋₆H₂O. The weight ratio of every component of the catalyst gained was K₂MoO₄/CoO/Co—SiO₂=15/1/(1.5-100). The evaluation result of the catalyst thus prepared is also shown in table 4

Example 17

The catalyst was prepared according to the experiment steps described in Example 1, but 0.45 g K₂MoO₄ and 0.5 g tartaric acid were replaced by 3.00 g of (NH₄)₆Mo₇O₂₄.4H₂O plus 0.45 g of KNO₃ and 0.5 g of citric acid respectively. The weight ratio of every component of the catalyst gained was MoO₃/K₂O/(Ni—SiO₂)=11/4/(4-100). The evaluation result of the catalyst thus prepared is shown in table 5

Example 18

The catalyst was prepared according to the experimental steps described in Example 12, but 0.496 g K₂MoO₄ was replaced by 3.00 g of (NH₄)₆Mo₇O₂₄.4H₂O plus 0.22 g of K₂CO₃. The weight ratio of every component of the catalyst gained was MoO₃/K₂O/NiO/(Ni—SiO₂)=11/4/0.25/(1.5-100). The assay result of the catalyst thus prepared was shown in table 5.

TABLE 2 performance of catalysts K₂MoO₄/Ni—SiO₂ in examples 7-11 Selectivity, % CO examples K₂MoO₄/(Ni—SiO₂) CH₄ CH₃SH COS CO₂ CO₂/CH₃SH Conversion, % 7  5/(1.5-100) 0.0956 28.74 40.12 31.04 1.080 30.21 8 10/(1.5-100) 0.0353 38.13 28.64 33.20 0.871 43.15 9 15/(1.5-100) 0.0282 46.61 16.79 36.57 0.785 65.61 10 20/(1.5-100) 0.0339 35.96 33.47 30.23 0.841 58.96 11 25/(1.5-100) 0.0496 30.38 38.24 31.33 1.030 59.63

TABLE 3 performance of catalysts K₂MoO₄—NiO/Ni—SiO₂ in examples 10-11 Selectivity, % CO % examples catalysts CH₄ CH₃SH COS CO₂ CO₂/CH₃SH conversion 12 K₂MoO₄/NiO/(Ni—SiO₂) = 0.0257 37.63 19.94 42.40 1.127 69.26 25/1.7/(1.5-100) 13 K₂MoO₄/CoO/(Ni—SiO₂) = 0.0214 37.64 19.10 43.24 1.148 62.58 25/2.6/(1.5-100)

TABLE 4 performance of catalysts K₂MoO₄/Co—SiO₂ in examples 14-16 Selectivity, % CO % examples catalysts CH₄ CH₃SH COS CO₂ CO₂/CH₃SH conversion 14 K₂MoO₄/(Co—SiO₂) = 0.01675 42.42 17.05 40.51 0.9550 36.33 (15/4.4-100) 15 K₂MoO₄/NiO/(Co—SiO₂) = 0.01507 46.15 23.66 30.17 0.6538 24.77 15/1.0/(1.5-100) 16 K₂MoO₄/CoO/(Co—SiO₂) = 0.01459 35.74 16.91 34.33 0.7705 24.64 15/1/(1.5-100)

TABLE 5 performance of catalysts K₂MoO₄—NiO/Ni—SiO₂ in examples 17-18 Selectivity, % CO % examples catalysts CH₄ CH₃SH COS CO₂ CO₂/CH₃SH conversion 17 MoO₃/K₂O/(Ni—SiO₂) = 0.0226 45.57 19.91 34.22 0.7466 56.84 11/4/(4.4-100) 18 MoO₃/K₂O/NiO/Ni—SiO₂ = 0.0283 39.55 22.21 38.20 0.9658 60.32 11/4/0.25/(1.5-100) 

1. A catalyst comprising a) a support, consisting of a porous carrier and a metal A deposited thereon by electroless deposition on the carrier; b) a Mo—O—K based active component; and c) optionally an active promoter Me_(x)O_(y), chosen from the group of transition metal oxides or rare earth metal oxides or rare earth metal oxides, wherein x and y depend on the valence of the metal.
 2. The catalyst according to claim 1, wherein the weight ratios of the components are K₂MoO₄/Me_(x)O_(y)/metal A-carrier=(1-30)/(0.0-25.0)/(0.1-10.0)-100 or MoO₃/K₂O/Me_(x)O_(y)/metal A-carrier=(1-30)/(1-20)/(0.0-25.0)/(0.1-10.0)-100
 3. The catalyst according to claim 2 wherein the weight ratios are K₂MoO₄/Me_(x)O_(y)/metalA-carrier=(15-20)/(0.0-25.0)/(0.5-8.0)-100; or MoO₃/K₂O/Me_(x)O_(y)/metalA-carrier=(15-20)/(10-15)/(0.0-25.0)/(0.5-8.0)-100.
 4. The catalyst according to claim 1, wherein the active promoter is an oxide selected from a group comprising the oxides of iron, cobalt, nickel, manganese, lanthanum and cerium.
 5. The catalyst according to claim 1, wherein said support is a material of metal(or metals)-plated carrier, which is defined as metal(or metals)-carrier, the weight ratio of metal(or metals)/carrier is metal(or metals)/carrier=(0.1-10.0)/100, preferably (0.5-8.0)/100.
 6. The catalyst according to claim 1, wherein said carrier is chosen from the group comprising SiO₂, TiO₂, Al₂O₃—SiO₂, zeolites, nano-carbon tubes or mixtures thereof.
 7. The catalyst according to claim 1, wherein the metal plated on the carrier is selected from transition metals, preferably from Ni, Co or Fe.
 8. The catalyst according to claim 1, wherein the support comprises reduced Pd and P components.
 9. Method of producing a catalyst comprising a porous support wherein a catalytically active component is deposited, characterised in that the method comprises the steps: a) activating a carrier, wherein the activation comprises the steps of first treating the carrier with a solution of a Pd-component and a reducing agent; b) impregnating said treated carrier with a solution comprising a solution of a metal salt whereby the metal is chosen from the group comprising Fe, Co, Ni, to achieve electroless deposition of said metal on the treated carrier to produce the catalyst support; c) impregnating said support with an impregnation liquid of an aqueous solution of K₂MoO₄ or (NH₄)Mo₇O₂₄ plus a potassium compound or MoO₃ plus a potassium compound; and optionally a precursor of said active promoter Me_(x)O_(y), followed by drying the received product to obtain the desired catalyst.
 10. The process according to claim 9, wherein said support is prepared by electroless plating method, the preparation processes include: (i) the preparation of metal-plating solution: a given quantity of soluble metal salt chosen and a given quantity of coordinating agent are dissolved in given quantity of distilled water successively to produce a metal-plating solution, in which the concentration of the metal ion varies from 1 g/l to 20 g/l, preferably 5-7 g/l; keeping stirring for 10 minutes, then a given quantity of a stabilizing agent are added one after another to the plating solution obtained above, stirring for another 20 minutes, followed by adding some NH₃.H₂0 to adjust the pH of the plating solution to 7.0-13.0, preferably 8.0-12.0; finally, suitable amount of distilled water is used to adjust the volume of the solution in such a way that the concentration of metal salt chosen in the plating solution varies from 1 g/l to 20 g/l, preferably 5-7 g/l. (ii) pretreatment of carrier chosen comprising the steps of a) the carrier should be washed with distilled water, and then dried, followed by treatment of the clean carrier by immersing it into a solution of 4.5 mol/1H₂SO₄+0.88 mol/1H₂0₂ (1:1) for 5 minutes under agitating, and then washed with distilled water three times; b) the cleaned carrier is immersed in an aqueous solution of activation agent under agitation, said activation agent is PdCl₂/HCl, the concentration of the activation agent varies from 0.05 g/l to 1.0 g/l, preferably from 0.1 g/l to 0.5 g/l; keeping ultrasonically agitating for 30-35 minutes, then washed with distilled water three times; c) the activated carrier is immersed in an aqueous solution of reduction agent under agitation, the concentration of the reduction agent varies from 20 g/l to 30 g/l, keeping agitating for 10 seconds; (iii) plating of metal onto carrier is conducted by putting the activated carrier produced in step (2) into the plating solution at 30-90° C. for 30-40 minutes. The metal-platted carrier is washed with distilled water three times and then dried at 110° C. for 6 hours.
 11. The process according to claim 9, wherein said reduction agent is NaH₂PO₃.H₂O or NaBH₄.
 12. The process according to claim 9, wherein said stabilizing agent is ammonium sulfate or ammonium chloride.
 13. The process according to claim 9, wherein said coordinating agent is at least one chosen from Na₃C₆H₅O₇.2H₂O, C₆H₈O₇.H₂O, C₂H₈N₂ or NaKC₄H₄O₆.4H₂O, the concentration of the chelating agent varies from 1 g/l to 60 g/l.
 14. The process according to claim 9, wherein the pH value of the electroless plating solution varies from 7.0 to 13.0, preferably from 8.0 to 12.0.
 15. The process according to claim 10, wherein at least one chelating reagent should present in the impregnation solution.
 16. The process according to claim 10, wherein the chelating reagent is chosen from the group of citric acid, ammonium citrate tribasic, L-glutamic acid, tartaric acid and ethylenediaminetetraacetic acid(EDTA); and the amount of chelating agent added correspondingly is 0.1-0.6 times as much as that of the support, more preferably is 0.3-0.6 times as much as that of the support.
 17. The process according to claim 9, wherein the pH value of the impregnation solution is adjusted to 8-12, preferably 8-10 by ammonia.
 18. The process according to claim 9, wherein the active promoter is an oxide selected from the group comprising the oxides of iron, cobalt, nickel, manganese, lanthanum and cerium.
 19. The process according to claim 9, wherein the weight ratio of the components of the obtained catalyst is K₂MoO₄/Me_(x)O_(y)/metal-carrier=(1-30)/(0.0-25.0)/(0.1-10.0)-100, when potassium molybdate is used as precursor or the weight ratio of the components of the catalyst is MoO₃/K₂O/Me_(x)O_(y)/metal-carrier=(1-30)/(1-20)/(0.0-25.0)/(0.1-10.0)-100, when (NH₄)₆Mo₇O₂₄.4H₂O plus one of potassium salts or MoO₃ plus one of potassium salts are used as precursors.
 20. The process according to claim 9, wherein the weight ratio of the components of the obtained catalyst is K₂MoO₄/Me_(x)O_(y)/metal-carrier=(15-20)/(0.0-25.0)/(0.5-8.0)-100, when potassium molybdate is used as precursor or the weight ratio of the contents of the catalyst is MoO₃/K₂O/Me_(x)O_(y)/metal-carrier=(15-20)/(10-15)/(0.0-25.0)/(0.5-8.0)-100; when (NH₄)₆Mo₇O₂₄.4H₂O plus one of potassium salts or MoO₃ plus one of potassium salts are used as precursors.
 21. A method for preparing methyl mercaptan in a catalytic process by reacting carbon oxides, sulphur and/or hydrogen sulphide, and hydrogen, comprising: a) providing a supported catalyst comprising a metal plated carrier, a Mo compound as active component and a promoter according to claim 1; and b) using said catalyst in the catalytic process. 